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LETM1 antibody detects LETM1 protein at cytoplasm on mouse stomach by immunohistochemical analysis. Sample: Paraffin-embedded mouse stomach. LETM1 antibody (GTX112455) diluted at 1:500. Antigen Retrieval: Trilogy? (EDTA based, pH 8.0) buffer, 15min
LETM1 antibody detects LETM1 protein at cytoplasm on mouse stomach by immunohistochemical analysis. Sample: Paraffin-embedded mouse stomach. LETM1 antibody (GTX112455) diluted at 1:500. 
 Antigen Retrieval: Trilogy? (EDTA based, pH 8.0) buffer, 15min
LETM1 antibody detects LETM1 protein at cytoplasm on mouse stomach by immunohistochemical analysis. Sample: Paraffin-embedded mouse stomach. LETM1 antibody (GTX112455) diluted at 1:500. Antigen Retrieval: Trilogy? (EDTA based, pH 8.0) buffer, 15min

LETM1 antibody

GTX112455
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetLETM1
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Overview

  • Supplier
    GeneTex
  • Product Name
    LETM1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3954
  • Target name
    LETM1
  • Target description
    leucine zipper and EF-hand containing transmembrane protein 1
  • Target synonyms
    CONDMIM, KHE, Mdm38, SLC55A1, mitochondrial proton/calcium exchanger protein, LETM1 and EF-hand domain-containing protein 1, mitochondrial, Mdm38 homolog, electroneutral mitochondrial K(+)/H(+)exchanger, leucine zipper-EF-hand containing transmembrane protein 1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO95202
  • Protein Name
    Mitochondrial proton/calcium exchanger protein
  • Scientific Description
    This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    41116161